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Research 91–120 of 1000+
- Six SNPs and a TTG indel in sheep desmoglein 4 gene are in complete linkage disequilibrium
- A computationally inferred regulatory heart aging model including post-transcriptional regulations
- Melanocytes and Vitiligo (and Hair Graying)
- Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia
- Woodhouse-Sakati syndrome: genotype–phenotype review and case of intra-familial heterogeneity
- Factors associated with early-onset androgenetic alopecia: A scoping review
- Dutasteride Micro-Injections in Androgenetic Alopecia
- Polycystic Ovary Syndrome in Adolescents
- Genetic Variation in the Human Androgen Receptor Gene Is the Major Determinant of Common Early-Onset Androgenetic Alopecia
- Androgens and androgen receptor action in skin and hair follicles
- Androgenic Alopecia Is Associated with Less Dietary Soy, Higher Blood Vanadium and rs1160312 1 Polymorphism in Taiwanese Communities
- Correlation between sebum level and severity of male androgenetic alopecia
- Hormonal regulation in male androgenetic alopecia—Sex hormones and beyond: Evidence from recent genetic studies
- Improving translational research in sex-specific effects of comorbidities and risk factors in ischaemic heart disease and cardioprotection: position paper and recommendations of the ESC Working Group on Cellular Biology of the Heart
- Genetic, hormonal and metabolic aspects of PCOS: an update
- Polycystic Ovary Syndrome
- Physiology of the Hypothalamic Pituitary Gonadal Axis in the Male
- Alopecia areata: An update
- Delivery of Tissue-Targeted Scalpels: Opportunities and Challenges for <i>In Vivo</i> CRISPR/Cas-Based Genome Editing
- A position effect on TRPS1 is associated with Ambras syndrome in humans and the Koala phenotype in mice
- 5α-Reduced glucocorticoids: a story of natural selection
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- Current evaluation of amenorrhea
- Evaluation of the predictive capacity of DNA variants associated with straight hair in Europeans
- MOUSE MODELS FOR THE STUDY OF HUMAN HAIR LOSS
- The Genetics of Human Skin Disease
- Alopecia Areata
- Integrative analysis of rare copy number variants and gene expression data in alopecia areata implicates an aetiological role for autophagy
- Skin diseases in consequence of endocrine alterations
- Clinical-exome sequencing unveils the genetic landscape of polycystic ovarian syndrome (PCOS) focusing on lean and obese phenotypes: implications for cost-effective diagnosis and personalized treatment